Legionnaires’ disease from a cooling tower in a community outbreak in Lidköping, Sweden- epidemiological, environmental and microbiological investigation supported by meteorological modelling
© Ulleryd et al.; licensee BioMed Central Ltd. 2012
Received: 28 March 2012
Accepted: 15 November 2012
Published: 21 November 2012
An outbreak of Legionnaires’ Disease took place in the Swedish town Lidköping on Lake Vänern in August 2004 and the number of pneumonia cases at the local hospital increased markedly. As soon as the first patients were diagnosed, health care providers were informed and an outbreak investigation was launched.
Classical epidemiological investigation, diagnostic tests, environmental analyses, epidemiological typing and meteorological methods.
Thirty-two cases were found. The median age was 62 years (range 36 – 88) and 22 (69%) were males. No common indoor exposure was found. Legionella pneumophila serogroup 1 was found at two industries, each with two cooling towers. In one cooling tower exceptionally high concentrations, 1.2 × 109 cfu/L, were found. Smaller amounts were also found in the other tower of the first industry and in one tower of the second plant. Sero- and genotyping of isolated L. pneumophila serogroup 1 from three patients and epidemiologically suspected environmental strains supported the cooling tower with the high concentration as the source. In all, two L. pneumophila strains were isolated from three culture confirmed cases and both these strains were detected in the cooling tower, but one strain in another cooling tower as well. Meteorological modelling demonstrated probable spread from the most suspected cooling tower towards the town centre and the precise location of four cases that were stray visitors to Lidköping.
Classical epidemiological, environmental and microbiological investigation of an LD outbreak can be supported by meteorological modelling methods.
The broad competence and cooperation capabilities in the investigation team from different authorities were of paramount importance in stopping this outbreak.
KeywordsLegionnaires’ disease Outbreak Epidemiology Cooling tower Meteorological computer models Sequence based typing
In 1976 at the American Legion Convention in Philadelphia, US, a severe pneumonia struck 182 of the attendees of which 29 where fatal . The disease was called Legionnaires’ disease (LD) and the bacterium was named Legionella pneumophila.
Numerous community-acquired outbreaks have been published, mostly emanating from cooling towers. Meteorological factors such as wind, humidity, and dispersion modelling were also discussed [4–11]. The only other known Swedish outbreak from a cooling tower also occurred in a hot and humid summer .
Three patients with clinically suspected Legionella pneumonia were reported 19 August 2004 by the clinicians at the Department of Medicine, Lidköping Hospital and the Consultants from the Department of Infectious Disease, Skövde Hospital to the Department of Communicable Disease Control and Prevention, Region Västra Götaland, a region with 1.5 million inhabitants. All three patients were living in Lidköping, a town with 38 000 inhabitants situated at river Lidan nearby the large Lake Vänern. The clinical suspicion of Legionnaires’ disease was based on non-responsiveness on initial standard betalactam treatment and further confirmed by urinary antigen test in two of the patients. Also, during the first half of August the hospital in Lidköping noticed a considerable increase of admissions of pneumonia patients. Health-care providers were informed about the possibility of an outbreak with LD, patient interviews and environmental sampling in the patients’ homes started, and localization of cooling towers and other aerosol producing installations began.
On 29 August a total of nine patients with a confirmed LD had been identified and next day an extended outbreak investigation team was formed with participation from the authors’ respective departments.
The objective of this report was to describe the outbreak from an epidemiological point of view and how the workup with identifying the source in order to stop the current outbreak was organised.
A person living in or visiting Lidköping between 1 August and 13 September 2004 seeking medical attention with clinical symptoms suggestive of LD plus clinically or radiologically verified pneumonia was considered as a presumptive case. Presumptive cases were identified in Lidköping Hospital, Skövde Hospital, primary health care centers in Lidköping and the mandatory Swedish notification system of communicable diseases. Furthermore, a positive sputum culture or urinary antigen test was defined as a confirmed LD case. A serological ≥ fourfold change in Legionella antibody titre or a single antibody titre of at least 1/128 in this outbreak setting was also defined as a confirmed LD case. A serological rise to a titre of 1/64 was defined as a presumptive LD case. Confirmed and presumptive cases were included in the total number of Legionella cases.
Respiratory specimens were cultured on non-selective and selective Buffered Charcoal Yeast Extract agar (BCYEα and MWY). Isolated Legionella strains were tested for species and serogroups. Urinary antigen tests were performed using Binax NOW ICT for detection of L. pneumophila serogroup (sg) 1 antigen. Serology for detection of Legionella antibodies was performed simultaneously using an indirect immunofluorescent technique (IFAT) with in-house prepared antigens by Section of Clinical Microbiology, Uppsala University Hospital.
Patients were interviewed according to a structured questionnaire including known risk factors for acquiring LD. The interviews were performed face to face by trained personnel with local knowledge of Lidköping. A map divided in small square fields was used to pinpoint where in the city the patients had been within 14 days before onset of symptoms. Repeated interviews were needed for patients with cerebral confusion and relatives were sometimes asked to complete the interviews.
The temperature was measured and samples were taken of the water in the homes by the Environmental Health Office personnel and if necessary advice of action was given. Public water reservoirs were also inspected and sampled. Possible industrial sources for Legionella, mainly cooling towers, were investigated.
Water samples from showers were analyzed by membrane filtration technique and incubated in 36°C on MWY-agar (Oxoid) for 7–10 days according to ISO standard 11731–2. Samples from cooling towers were analyzed in 10-fold series after acid treatment and further spread on MWY-agar. A latex agglutination test with Dryspot (Oxoid) directly from the agar plate was used after two days incubation for the cooling tower samples for preliminary identification.
Bacterial isolates were cultured on BCYEα agar at 35°C for 3 days before testing.
Serological typing was performed using the Dresden panel of monoclonal antibodies (MAb) . The genetic profile of patient isolates was compared to that of environmental isolates using sequence-based typing (SBT) using the genes fla A, pil E, asd , mip , momp S, pro A, neu A. A consensus method has been validated and a database for sequence type (ST) set up by The European Working Group for Legionella Infections (EWGLI) .
Weather reports from nearby Såtenäs airport were assessed. ALARM (Advanced Local And Regional Modelling system), a model for spread from a point source using a combination of measurements and a database of simulated wind and turbulence fields was used, where the topography of the terrain is also included [14–17]. This system is implemented in Region Västra Götaland including three SODAR (sonic detection and ranging) plants and 10 mast measuring points. The main purpose of ALARM is to help the authorities predict spread of toxic substances, for example in case of a chemical accident.
The work in this paper was part of an outbreak investigation. The regional departments of communicable disease control and prevention in Sweden have general consent to conduct outbreak investigations and contact tracing is routine. This is regulated by the Swedish Communicable Diseases Act (2004) and includes interviews, testing, epidemiological investigations, communicating results of the investigation etc. A specific approval for the work presented was therefore not needed in this outbreak setting.
The purpose of this work was to identify the cause of the outbreak and to implement interventions to prevent further cases, also preventing future outbreaks-to-be. Therefore, this report was not considered to be research and was therefore exempt from human subjects review.
Cases and microbiological investigation
All diagnostic procedures were not performed in all patients. Sputum culture, urinary antigen test, and serology for Legionella were performed in 50, 72, and 97 patients respectively.
Three cases grew L. pneumophila sg 1. Twelve other cases showed a positive urinary antigen test for L. pneumophila. Of these, in all 15 patients, 14 were available for serological testing. Six cases showed a significant titre change or a single high titre ≥ 128, one was presumptive with a titre of 64 and seven were negative.
Additionally, nine patients were found to be serologically confirmed cases. Another eight patients were presumptive serologically positive and included as LD cases according to the case definition. The total number of confirmed and presumptive LD cases was 32.
The median age of the 32 cases was 62 years (range 36–88) with 22 (69%) males. Other personal risk-factors found were current tobacco smoking in 22 (69%) and severe medical illness in 12 (38%) of the patients. All patients presented with a temperature ≥ 38.0°C, 23 (72%) had symptoms of central nervous system engagement, 17 (53%) had cough and gastrointestinal symptoms, and two were submitted to assisted ventilation. Two cases died, giving a mortality rate of 6%. A detailed report on case characteristics, diagnostic yield and clinical course for the 32 confirmed and presumptive LD cases have been published separately .
Twenty-one of the 32 cases lived in central Lidköping, seven were frequent visitors and lived in the municipal periphery, and four of the patients had only visited the municipality of Lidköping at one time within a 2–10 day period before onset of their symptoms. No common indoor exposure was found in the interviews. None of the patients confirmed any contact with whirlpools, car-washing facilities, air humidifiers/air conditioning devices at home or home-fountains.
A total of 61 environmental samples for Legionella were processed. Initially, investigations of the showers grew Legionella in two of six patient homes with 3500 and 150 cfu/L respectively, in the samples taken after flushing. The identification showed other serotypes than found among patient isolates. In a mist machine for vegetables at the supermarket (Figure 2), a concentration of 79 000 cfu/L of L. pneumophila sg 1 was found. This device had been out of use for 4 days when sampled and the amount of bacteria found in the sample does not reflect the situation when it was in use.
All cooling towers in the city, fifteen towers in eight industries, were sampled for culture. Outdoor fountains and drinking water were negative.
Three cooling towers from two industries (A and B) were positive for L. pneumophila sg 1. After only 48 hours incubation of the first samples from the suspected Industry A, cooling tower 1 we spotted thousands of Legionella colonies and a latex agglutination test was positive for L. pneumophila sg 1. Further quantification showed growth of 1 200 000 000 cfu/L. The other two positive cooling towers had concentrations of Legionella between 100 000 – 600 000 cfu/L, all of them exceeding the upper action limit given by EWGLI at 10 000 cfu/L .
Legionella outbreak isolates from patients and environment in Lidköping 2004
Legionella cfu per L
Legionella pneumophila serogroup
Monoclonal subtype (Dresden panel)
Seven gene SBT (flaA, pilE, asd, mip, mompS, proA, neuA)
Cooling tower 1, Industry A
400 000 000*
800 000 000*
Cooling tower 2, Industry A
Cooling tower 3, Industry B
Cooling tower 4, Industry B
Shower at home Patient II
Shower at home Patient III
The two patient Benidorm (I, II) isolates (ST639) were genotypically quite different from the patient Bellingham (III) isolate (ST59). Both STs could be found in the suspected cooling towers of Industry A, which was suspected as a source of infection. However, the environmental isolate that was genotypically identical with the patient Bellingham strain reacted as a Benidorm using the MAb panel. It has been shown previously that Benidorm and Bellingham strains that have identical genetic profiles may occur in the same water system . Based on the ST we regard Industry A/cooling tower 2 as the likely source of the infection in the patient with the Lp1/Bellingham/ST59 strain.
The two cooling towers at Industry A were closed 3 September and decontaminated. Industry B closed their cooling towers for decontamination 4 September. These decisions were based on the finding of the huge growth in one of the cooling towers, the patient information of an intermittent unpleasant smell blowing in the wind from a power plant adjacent to Industry A, and the four stray visitors. The last onset of symptoms of a confirmed case was 13 September, within the incubation time (Figure 1).
Initially, there was a certain fear and pressure from the public and media on the authorities for some kind of action. No general closing or other action was taken until 3 September. The progress of the investigation was thoroughly reported in press releases, put together by the investigation team at telephone conferences on a regular basis, first every two days, and later more infrequent. Questions regarding the environmental investigation were answered by one person at the local Environmental Health Office and questions about the disease or the patients were answered by one specified person from the Department of Communicable Disease Control and Prevention. A lot of telephone calls from the public were also answered by respective authority and the local healthcare.
An industrial cooling tower was the probable source for this Legionella outbreak with aerosol spread that included at least 32 patients with two fatal outcomes. The cooling tower was of the open-type without a drip-eliminator where condensed steam was released with a very high concentration of L. pneumophila sg 1, subtype Benidorm belonging to the virulent MAb 3–1 group.
There was a concomitant increase in patients with lower respiratory tract infections, the majority of these admitted to hospital (Figure 1). It is evident in this study that not all true cases are found or detected with our standard diagnostic tests, which has also been discussed in earlier LD outbreak reports [5, 6]. After recognition of the outbreak 19 August, there was an increased tendency of the public to attend healthcare and the alertness possibly rendered more patients with suspected pneumonia to be admitted to hospital. This phenomenon could at least to some extent explain the second peak. However, much of the surplus of pneumonia cases compared to the expected incidence could represent LD cases not confirmed by the available diagnostic tests. The importance of informing the public in outbreak management is pointed out in another report .
One limitation of this investigation is that no case–control analysis was done. Such a study was initially discussed but refrained from mainly two reasons. First, it could be difficult to find a control group in this epidemic that was spread in all Lidköping of a disease where possibly only one in 1000 exposed will contract the disease . Second, the time and effort in performing a case–control analysis would possibly jeopardize a fast finding and closing of the source.
Legionella culture from sputum was positive in three cases out of 50 cultures sampled from 106 patients. As the first wave of onset of lower respiratory tract infection already peaked before the recognition of the outbreak (Figure 1), a lot of emphasis of the clinicians was put in obtaining these cultures. An early identification of patient isolates is crucial for the epidemiological typing comparison with available environmental isolates. But, given the low diagnostic yield, sputum culture for confirmation of LD has limited importance from a clinical point of view compared to the urinary antigen test and sputum PCR test if available.
The patient interviews were time-consuming as many of the patients experienced some degree of confusion. A very good local knowledge of the interviewers was of importance, particularly in the mapping of where the patients had been during the 14 days prior to onset of symptoms. As described in most outbreaks, the majority of the patients were elderly, males, and tobacco smokers [2, 3].
Finding “outlaying cases” such as the four stray visitors in Lidköping was of great help in the epidemiological investigation, and later combined with the wind modelling, reinforced the data presented from the environmental cultures and typing.
The finding of positive Legionella cultures from the environment is expected. A mixture of more than one Legionella species or subtype in the same sample is also common [3, 4]. The number of subtypes found in each sample was maybe underestimated in reports before modern genotyping methods were available . Another confounding factor in typing is the difficulties in selecting enough number of colonies from the primary culture. All typing methods have their advantages and disadvantages and each method contribute in its own way to the puzzle of linking patient- and environmental isolates to each other.
Both sequence types isolated from the patients and Industry A could also be found at other locations in Lidköping, possibly due to a common spread from open water or the water system into the surroundings, as expected according to other studies . Cooling tower 1 in Industry A had a remarkably high concentration of Legionella sg 1 ST639, making it the most probable source. The lower concentration of Legionella sg 1 ST59 in Industry B made it less likely as the source of the outbreak. ST639 is only found in Lidköping in the SBT database at EWGLI.
Meteorological investigation and modelling can provide important information about wind conditions as aerosol spread up to many kilometers have been reported [6–11]. Different types of dispersion modelling systems are quite widespread, mainly for scientific purposes or in case of chemical or radioactive pollution.
The probable date of infection for the index cases in our investigation coincided with a change from a chilly to a rather warm humid weather, which may have played a role in the spread of the Legionella bacteria from the cooling tower. Some reports have stated that it is the humidity, not the heat, which increases the risk for LD outbreaks . Comparing the airport weather data did not give any clear-cut explanation of the two-spiked epidemic curve. It has been suggested that high temperatures and high humidity can influence infective nuclei in an aerosol to spread more easily . Other factors such as biological material within aerosol-producing water sources and biofilm production may be of importance preceding an outbreak . We did notice a lot of biofilm formation inside and on the cooling tower 1 at Industry A and also on the walls of the surrounding buildings.
Outbreak investigation is always a race against time. The outbreak investigation team has to gather as many facts as possible in a short time to be able to draw a conclusion of the most probable source or sources of the outbreak. The closing or elimination of the probable source must often be expedited without waiting for all results of sampling. All in order to avoid further cases without unnecessary disturbing normal social life and enterprise. The first 48 hours after notification of a LD outbreak have been reported to be very important .
Classical epidemiological, environmental and microbiological investigation of an LD outbreak can be supported by meteorological modelling methods.
A steady alertness for unexpected clustering of clinical cases, prompt organization of the investigation team, and a smoothly running cooperation of all included stakeholders such as the health-care, local-regional-national authorities, the public, the media, and the private enterprise were factors that facilitated the relatively fast finding and closing of the source for this outbreak. After the outbreak, an intense activity of industries all over Sweden started regarding the maintenance and control of existing cooling towers such as already existing in other countries .
Sverker Bernander Deceased
Thanks to David Svenson, Luft i Väst for fruitful cooperation, Leif Larsson and co-workers, Clinical Bacteriology, Sahlgrenska University Hospital for laboratory help and Eva Hjelm, Clinical Microbiology, Uppsala University Hospital for serological typing. Dr. Jürgen Helbig, Dresden, Germany, kindly confirmed the results of subgrouping patient isolates and a few environmental isolates from suspected sources.
- Fraser DW, Tsai TR, Orenstein W, Beecham HW, Harris J, Sharrar RJ, Harris J, Mallison GF, Martin SM, McDade JE, Shepard CC, Brachman PS: Legionnaires’ disease: description of an epidemic of pneumonia. N Engl J Med. 1977, 297: 1189-1197. 10.1056/NEJM197712012972201.View ArticlePubMedGoogle Scholar
- Legionellosis. Control of Communicable Diseases Manual. 18th edition. Edited by: Heymann DL. 2004, Washington: American Public Health AssociationGoogle Scholar
- EWGLI homepage: [http://www.ewgli.org]
- Nordström K, Kallings I, Dahnsjö H, Clemens F: An outbreak of legionnaires’ disease in Sweden: report of sixty-eight cases. Scand J Infect Dis. 1983, 15: 43-45.View ArticlePubMedGoogle Scholar
- García-Fulgueiras A, Navarro C, Fenoll D, García J, González-Diego P, Jiménez-Buñuales T, Rodriguez M, Lopez R, Pacheco F, Ruiz J, Segovia M, Balandrón B, Pelaz C: Legionnaires’ disease outbreak in Murcia, Spain. Emerg Infect Dis. 2003, 9: 915-921.View ArticlePubMedPubMed CentralGoogle Scholar
- Sabria M, Alvarez J, Dominguez A, Pedrol A, Sauca G, Salleras L, Lopez A, Garcia-Nuñez MA, Parron I, Barrufet MP: A community outbreak of Legionnaires’ disease: evidence of a cooling tower as the source. Clin Microbiol Infect. 2006, 12: 642-647. 10.1111/j.1469-0691.2006.01447.x.View ArticlePubMedGoogle Scholar
- Nguyen TM, Ilef D, Jarraud S, Rouil L, Campese C, Che D, Haeghebaert S, Ganiayre F, Marcel F, Etienne J, Desenclos JC: A community-wide outbreak of legionnaires’ disease linked to industrial cooling towers - how far can contaminated aerosols spread?. J Infect Dis. 2006, 193: 102-111. 10.1086/498575.View ArticlePubMedGoogle Scholar
- Blystad H, Brantsæter AB, Løvoll O: Outbreak of community-acquired legionnaires’ disease in southeast Norway, May 2005. Euro Surveill. 2005, 10: E050526.-PubMedGoogle Scholar
- Nygård K, Werner-Johansen Ø, Rønsen S, Caugant DA, Simonsen Ø, Kanestrøm A, Ask E, Ringstad J, Ødegård R, Jensen T, Krogh T, Høiby EA, Ragnhildstveit E, Aaberge IS, Aavitsland P: An outbreak of Legionnaires’ disease caused by long-distance spread from an industrial air scrubber in Sarpsborg. Norway. Clin Infect Dis. 2008, 46: 61-69.View ArticlePubMedGoogle Scholar
- Sala Ferré MR, Arias C, Oliva JM, Pedrol A, García M, Pellicer T, Roura P, Domínguez A: A community outbreak of Legionnaires’disease associated with a cooling tower in Vic and Gurb, Catalonia (Spain) in 2005. Eur J Clin Microbiol Infect Dis. 2009, 28: 153-159. 10.1007/s10096-008-0603-6.View ArticleGoogle Scholar
- Castilla J, Barricarte A, Aldaz J, García Cenoz M, Ferrer T, Pelaz C, Pineda S, Baladrón B, Martín I, Goñi B, Aratajo P, Chamorro J, Lameiro F, Torroba L, Dorronsoro I, Martínez-Artola V, Esparza MJ, Gastaminza MA, Fraile P, Aldaz P: A large Legionnaires’ disease outbreak in Pamplona, Spain: early detection, rapid control and no case fatality. Epidemiol Infect. 2008, 136: 823-832.View ArticlePubMedGoogle Scholar
- Helbig JH, Kurtz JB, Castellani-Pastoris M, Pelaz C, Lück PC: Antigenic polysaccharide components of Legionella pneumophila recognized by monoclonal antibodies: possibilities and limitations for division of the species into serogroups. J Clin Microbiol. 1997, 35: 2841-2845.PubMedPubMed CentralGoogle Scholar
- Gaia V, Fry NK, Afshar B, Lück PC, Meugnier H, Etienne J, Peduzzi R, Harrison TG: Consensus sequence-based scheme for epidemiological typing of clinical and environmental isolates of Legionella pneumophila. J Clin Microbiol. 2005, 43: 2047-2052. 10.1128/JCM.43.5.2047-2052.2005.View ArticlePubMedPubMed CentralGoogle Scholar
- Enger L: Simulation of dispersion in moderately complex terrain - part C. A dispersion model for operational use. Atmos Environ. 1990, 24A: 2457-2471. Part-AView ArticleGoogle Scholar
- Enger L: Simulation of dispersion in moderately complex terrain. Air pollution modeling and its application VIII. (Plenum, with NATO; Challenges of Modern Society, 15). 1991, 321-328.Google Scholar
- Melas D, Enger L: A numerical study of flow in Athens area using the MIUU model. Environ Softw. 1993, 8: 55-63. 10.1016/0266-9838(93)90008-6.View ArticleGoogle Scholar
- Luft i Väst homepage: [http://www.luftivast.se]
- Hugosson A, Hjorth M, Bernander S, Claesson BE, Johansson A, Larsson H, Nolskog P, Pap J, Svensson N, Ulleryd P: A community outbreak of Legionnaires’ Disease from an industrial cooling tower: Assessment of clinical features and diagnostic procedures. Scand J Infect Dis. 2007, 39: 217-224. 10.1080/00365540601001930.View ArticlePubMedGoogle Scholar
- Helbig JH, Lück PC, Knirel YA, Witzleb W, Zähringer U: Molecular characterization of a virulence-associated epitope on the lipopolysaccharide of Legionella pneumophila serogroup 1. Epidemiol Infect. 1995, 115: 71-78. 10.1017/S0950268800058131.View ArticlePubMedPubMed CentralGoogle Scholar
- Darelid J, Bernander S, Jacobson K, Lofgren S: The presence of a specific genotype of Legionella pneumophila serogroup 1 in a hospital and municipal water distribution system over a 12-year period. Scand J Infect Dis. 2004, 36: 417-423. 10.1080/00365540410020749.View ArticlePubMedGoogle Scholar
- Fisman DN, Lim S, Wellenius GA, Johnson C, Britz P, Gaskins M, Maher J, Mittleman MA, Spain CV, Haas CN, Newbern C: It's not the heat, it's the humidity: wet weather increases legionellosis risk in the greater Philadelphia metropolitan area. J Infect Dis. 2005, 192: 2066-2073. 10.1086/498248.View ArticlePubMedGoogle Scholar
- Van Steenbergen JE, Slijkerman FA, Speelman P: The first 48 hours of investigation and intervention of an outbreak of legionellosis in the Netherlands. Euro Surveill. 1999, 4: 111-115.PubMedGoogle Scholar
- Rangel KM, Delclos G, Emery R, Symanski E: Assessing maintenance of evaporative cooling systems in legionellosis outbreaks. J Occup Environ Hyg. 2011, 8: 249-265. 10.1080/15459624.2011.565409.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/12/313/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.